Roundabout homolog 3 is a protein that in humans is encoded by the ROBO3 gene. [5] [6]
Conjugate gaze palsies are neurological disorders affecting the ability to move both eyes in the same direction. These palsies can affect gaze in a horizontal, upward, or downward direction. These entities overlap with ophthalmoparesis and ophthalmoplegia.
Aristaless related homeobox is a protein that in humans is encoded by the ARX gene.
The human gene SPAST codes for the microtubule-severing protein of the same name, commonly known as spastin.
Cell division cycle 73, Paf1/RNA polymerase II complex component, homolog , also known as CDC73 and parafibromin, is a protein which in humans is encoded by the CDC73 gene.
Sodium channel protein type 1 subunit alpha (SCN1A), is a protein which in humans is encoded by the SCN1A gene.
Aprataxin is a protein that in humans is encoded by the APTX gene.
Progressive ankylosis protein homolog is a protein that in humans is encoded by the ANKH gene.
Epsilon-sarcoglycan is a protein that in humans is encoded by the SGCE gene.
Probable helicase senataxin is an enzyme that in humans is encoded by the SETX gene.
Netrin-1 is a protein that in humans is encoded by the NTN1 gene.
Sodium channel subunit beta-1 is a protein that in humans is encoded by the SCN1B gene.
Alpha-1,2-mannosyltransferase ALG9 is an enzyme that in humans is encoded by the ALG9 gene.
EF-hand domain-containing protein 1 is a protein that in humans is encoded by the EFHC1 gene.
Fermitin family homolog 1 is a protein that in humans is encoded by the FERMT1 gene.
Hemicentin-1 is a protein that in humans is encoded by the HMCN1 gene.
Roundabout homolog 2 is a protein that in humans is encoded by the ROBO2 gene.
Myotubularin-related protein 13 is a protein that in humans is encoded by the SBF2 gene.
Protein O-mannosyl-transferase 2 is an enzyme that in humans is encoded by the POMT2 gene.
Rho-related BTB domain-containing protein 2 is a protein that in humans is encoded by the RHOBTB2 gene.
Spatacsin is a protein that in humans is encoded by the SPG11 gene.